JPS6056197B2 - hot melt adhesive composition - Google Patents
hot melt adhesive compositionInfo
- Publication number
- JPS6056197B2 JPS6056197B2 JP9387679A JP9387679A JPS6056197B2 JP S6056197 B2 JPS6056197 B2 JP S6056197B2 JP 9387679 A JP9387679 A JP 9387679A JP 9387679 A JP9387679 A JP 9387679A JP S6056197 B2 JPS6056197 B2 JP S6056197B2
- Authority
- JP
- Japan
- Prior art keywords
- nylon
- adhesive composition
- hot melt
- melt adhesive
- vinyl aromatic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Landscapes
- Adhesives Or Adhesive Processes (AREA)
Description
【発明の詳細な説明】
本発明はホットメルト型の接着剤組成物に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a hot melt adhesive composition.
従来より、ポリエチレン、エチレン酢酸ビニル共重合体
、アイオノマー、ナイロン等の熱可塑性樹脂を材料とす
るホットメルト型接着剤は多数知られている。Many hot-melt adhesives made from thermoplastic resins such as polyethylene, ethylene-vinyl acetate copolymers, ionomers, and nylon have been known.
しかし、ポリエチレン、エチレン酢酸ビニル共重合体、
アイオノマー等は金属などの接着に使用した場合充分な
接着強度が得られず実用に供し難かつた。However, polyethylene, ethylene vinyl acetate copolymer,
When ionomers and the like are used for adhering metals, etc., sufficient adhesion strength cannot be obtained, making it difficult to put them into practical use.
又、ナイロンについては金属に対し或る程度の接着強度
は有するがいまだ充分てなく、そのためナイロンにエポ
キシ樹脂等を配合したり、又は、ナイロンフィルムの両
面にエポキシ樹脂をコーティングしたいわゆるナイロン
−エポキシ系のホットメルト型接着剤が提案されている
が、この様な接着剤は硬化の完了にかなりの長時間を要
し、又、コスト的にも高くつくので、一般的な用。途の
接着剤としては適当でない。又、ナイロンにエチレン−
酢酸ビニル共重合体やアイオノマー等を混合することに
より接着強度を向上させようとする試みをなされている
が、いずれの場合も接着強度向上についての満足すべき
成果が得られておらず、さらに該強度の向上が望まれて
いる。本発明はかゝる現状にかんがみ、金属等に対する
接着強度にすぐれ、使いやすく、しかも安価なホットメ
ルト接着剤組成物を提供することを目的としてなされた
ものであり、その要旨はナイロン系重合体100重量部
に対してビニル芳香族炭化水−素の重合体が1〜20踵
量部混合されてなることを特徴とするホットメルト接着
剤組成物に存する。本発明においてナイロン系重合体と
は一般にナイロンと呼称されており、従来においてホッ
トメルト型接着剤として用いることが知られているたと
えばナイロン12、ナイロン11、ナイロン6、ナイロ
ン66、ナイロン610やこれらの共重合体を指すもの
である。Also, although nylon has a certain degree of adhesive strength to metals, it is not yet sufficient, so nylon is mixed with epoxy resin, or so-called nylon-epoxy adhesives, which are coated with epoxy resin on both sides of a nylon film, are used. Hot-melt adhesives have been proposed, but such adhesives require a considerable amount of time to complete curing and are expensive, so they are not suitable for general use. It is not suitable as a temporary adhesive. Also, ethylene on nylon
Attempts have been made to improve adhesive strength by mixing vinyl acetate copolymers, ionomers, etc., but in none of these cases has a satisfactory result been achieved in improving adhesive strength. Improvement in strength is desired. In view of the current situation, the present invention has been made for the purpose of providing a hot melt adhesive composition that has excellent adhesive strength to metals, etc., is easy to use, and is inexpensive. A hot melt adhesive composition characterized in that 1 to 20 parts by weight of a vinyl aromatic hydrocarbon polymer is mixed with 100 parts by weight. In the present invention, the nylon polymer is generally referred to as nylon, and includes nylon 12, nylon 11, nylon 6, nylon 66, nylon 610, etc., which are conventionally known to be used as hot melt adhesives. It refers to a copolymer.
又、ビニル芳香族炭化水素の重合体とは重合可能なビニ
ル芳香族炭化水素単量体の単独重合体か或いは該ビニル
芳香族炭化水素単量体を主体とする他の重合性単量体と
の共重合体を指す。In addition, the polymer of vinyl aromatic hydrocarbon refers to a homopolymer of a polymerizable vinyl aromatic hydrocarbon monomer, or a polymer of other polymerizable monomers mainly composed of the vinyl aromatic hydrocarbon monomer. refers to a copolymer of
そして本発明において通常炭素数8〜20のビニル芳香
族炭化水素の単独重合体或は共重合体、例えばポリスチ
レン、ポリα−メチルスチレン、ポリビニルトルエン、
ポリβ−メチルスチレン、ポリターシヤリーブチルスチ
レン、ポリイソプロペニルトルエン等が好適に用いられ
、特にポリスチレンが好適に用いられる。本発明接着剤
組成物を製造するには前記ナイロン系重合体と前記ビニ
ル芳香族炭化水素の重合体とを加え合せて混合して適宜
な形状のものとすればよく、例えばこれらの重合体の粉
末或いはペレット状のものを混合して、押出機にかけフ
ィルム状、線状、ペレット状に成形するとか、ロール、
ニーダー、パンバリーミキサー等により混練しシート状
等に成形する方法が好適に採用出来る。In the present invention, homopolymers or copolymers of vinyl aromatic hydrocarbons having 8 to 20 carbon atoms, such as polystyrene, polyα-methylstyrene, polyvinyltoluene,
Polyβ-methylstyrene, polytert-butylstyrene, polyisopropenyltoluene, etc. are preferably used, and polystyrene is particularly preferably used. To produce the adhesive composition of the present invention, the nylon polymer and the vinyl aromatic hydrocarbon polymer may be added and mixed to form an appropriate shape. Mix powder or pellets and use an extruder to form them into a film, line, or pellet, or roll,
A method of kneading with a kneader, Panbury mixer, etc. and forming it into a sheet shape or the like can be suitably employed.
そして、前記ナイロン系重合体とビニル芳香族炭化水素
の重合体との使用量については、前者10喧量部に対し
て後者を1〜20喧量部の範囲で用いることを必要とす
る。その理由は、ビニル芳香族炭化水素の重合体の使用
量が1重量部未満の場合は得られる接着剤組成物の剥離
強度の増大という効果が発現されず、20鍾量部を越え
る場合は、ナイロン系重合体との混和性の限界を越える
ためと推測されるが、剥離強度が低下する傾向にあるか
らである。As for the amounts of the nylon polymer and the vinyl aromatic hydrocarbon polymer, it is necessary to use the latter in a range of 1 to 20 parts by weight per 10 parts by weight of the former. The reason for this is that if the amount of the vinyl aromatic hydrocarbon polymer used is less than 1 part by weight, the effect of increasing the peel strength of the resulting adhesive composition will not be achieved, and if it exceeds 20 parts by weight, This is presumably because the limit of miscibility with the nylon polymer is exceeded, but the peel strength tends to decrease.
本発明接着剤組成物は一般のホットメルト接着剤と同様
な用途に使用されることが出来るが、特に鉄、アルミニ
ウム、銅、真ちゆうなどの金属材料、ガラス、陶磁器、
スレート、コンクリートなどの無機材料、木綿、絹、羊
毛、テトロン、ナイロン、繊維などの繊維材料や紙製品
などのを接着するのに使用されてすぐれた特性を発揮し
得る。The adhesive composition of the present invention can be used for the same purposes as general hot-melt adhesives, but in particular metal materials such as iron, aluminum, copper, and brass, glass, ceramics, etc.
It exhibits excellent properties when used to bond inorganic materials such as slate and concrete, fibrous materials such as cotton, silk, wool, Tetoron, nylon, and fibers, and paper products.
なお本発明接着剤組成物には、着色剤、充填剤等の添加
剤が必要に応じ加えられてもさしつかえない。本発明の
ホットメルト接着剤組成物は上述の通りの構成のもので
あるので、すぐれた接着強度を示すことが出来るもので
ある。Note that additives such as colorants and fillers may be added to the adhesive composition of the present invention as necessary. Since the hot melt adhesive composition of the present invention has the above-described structure, it can exhibit excellent adhesive strength.
以下本発明の実施例について説明する。Examples of the present invention will be described below.
実施例1〜2
共重合ナイロン(融点117℃、メルトインデックス3
5)とポリスチレン(ビスカット軟化点85℃、メルト
インデックス27)とを第1表に示す割合で配合し、押
出機により厚さ100ミクロンのフィルム状に押出して
、フィルム状接着剤となした。Examples 1-2 Copolymerized nylon (melting point 117°C, melt index 3
5) and polystyrene (Viscut softening point: 85° C., melt index: 27) in the proportions shown in Table 1, and extruded into a film with a thickness of 100 microns using an extruder to obtain a film adhesive.
次にこの接着剤をアセトン説脂した厚さ0.6TIr1
1tの2枚の亜鉛鋼板の間におき、温度120℃、加圧
2k9/C7lf、2分間の接着条件で該鋼板同志を接
着し、接着後2CfCで相対湿度60%の条件下に3日
間放置した。Next, this adhesive was greased with acetone to a thickness of 0.6TIr1.
Placed between two 1t galvanized steel plates, the steel plates were bonded together at a temperature of 120°C and a pressure of 2K9/C7lf for 2 minutes. After bonding, the steel plates were left for 3 days at 2CfC and a relative humidity of 60%. did.
かくして接着された亜鉛鋼板のT剥離強度を測定した。The T-peel strength of the thus bonded galvanized steel sheets was measured.
測定条件は剥離速度50Wfi/分、サンプル巾25顛
、温度20℃、湿度60%であつた。T剥離強度の測定
結果を第1表に示す。実施例3〜4
ナイロン12(融点179
カツト軟化点85℃、メルトインデックス27)を第1
表に示す割合で配合し、実施例1と同様にして接着剤を
用意した。The measurement conditions were a peeling rate of 50 Wfi/min, a sample width of 25 pieces, a temperature of 20° C., and a humidity of 60%. Table 1 shows the measurement results of T peel strength. Examples 3-4 Nylon 12 (melting point 179, cutt softening point 85°C, melt index 27) was used as the first
An adhesive was prepared in the same manner as in Example 1 by blending in the proportions shown in the table.
次に接着を温度240℃、加圧2k9/Cril2分間
の条件で行う以外は実施例1と同様にして試料を用意し
、T剥離強度の測定を行つた。その結果は第1表に示さ
れる通りであつた。比較例1
共重合ナイロン(実施例1と同じ)を単独て用いて実施
例1と同様にして接着剤を用意し、T剥離強度を測定し
た。Next, a sample was prepared in the same manner as in Example 1 except that bonding was performed at a temperature of 240° C. and a pressure of 2K9/Criel for 2 minutes, and the T-peel strength was measured. The results were as shown in Table 1. Comparative Example 1 An adhesive was prepared in the same manner as in Example 1 using only copolymerized nylon (same as in Example 1), and the T-peel strength was measured.
その結果は第1表の通りであつた。The results were as shown in Table 1.
比較例2
ナイロン12(実施例3と同じ)を単独で用いて接着剤
とする以外は実施例5と同様にした。Comparative Example 2 The same procedure as in Example 5 was carried out except that nylon 12 (same as in Example 3) was used alone as an adhesive.
その結果は第2表の通りであつた。実施例5〜8、比較
例3〜4
実施例1と同様にして、第2表及び第3表に記載の組成
を有する接着剤を用意し、T剥離強度を測定した。The results were as shown in Table 2. Examples 5 to 8, Comparative Examples 3 to 4 In the same manner as in Example 1, adhesives having the compositions shown in Tables 2 and 3 were prepared, and the T-peel strength was measured.
その結果は表の通りであつた。尚、共重合ナイロン及び
ポリスチレンは実施例1と同じものを、ナイロン12は
実施例3と同じものを夫々用いた。The results were as shown in the table. The same copolymerized nylon and polystyrene as in Example 1 were used, and the same as in Example 3 was used as nylon 12.
Claims (1)
族炭化水素の重合体が1〜200重量部混合されてなる
ことを特徴とするホットメルト接着剤組成物。 2 ビニル芳香族炭化水素の重合体がポリスチレンであ
る第1項記載の組成物。Claims: 1. A hot melt adhesive composition comprising 1 to 200 parts by weight of a vinyl aromatic hydrocarbon polymer mixed with 100 parts by weight of a nylon polymer. 2. The composition according to item 1, wherein the vinyl aromatic hydrocarbon polymer is polystyrene.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9387679A JPS6056197B2 (en) | 1979-07-23 | 1979-07-23 | hot melt adhesive composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9387679A JPS6056197B2 (en) | 1979-07-23 | 1979-07-23 | hot melt adhesive composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5618670A JPS5618670A (en) | 1981-02-21 |
| JPS6056197B2 true JPS6056197B2 (en) | 1985-12-09 |
Family
ID=14094662
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9387679A Expired JPS6056197B2 (en) | 1979-07-23 | 1979-07-23 | hot melt adhesive composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6056197B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5422398A (en) * | 1993-04-23 | 1995-06-06 | The University Of Connecticut | Compatibilizer for polymer blends and the polymer blends derived therefrom |
-
1979
- 1979-07-23 JP JP9387679A patent/JPS6056197B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5618670A (en) | 1981-02-21 |
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